5ce0bdcca4ae369483d0aedd620fd6da

1. LIGHTMIX MODULAR ADENOVIRUS

TIB MOLBIOL SYNTHESELABOR GMBH·II·Colombia INVIMA·Expires August 30, 2032

Device classification

Risk class / Clase de Riesgo: II
Product type (Spanish): REACTIVO DIAGNOSTICO
Product type (English): DIAGNOSTIC REAGENT

Registration information

Analysis ID: 5ce0bdcca4ae369483d0aedd620fd6da
Expire date: August 30, 2032

Authorized company / Fabricante

Name (Spanish): TIB MOLBIOL SYNTHESELABOR GMBH
Name (English): TIB MOLBIOL SYNTHESELABOR GMBH

Product use / Uso del Producto

Spanish

DETERMINACIÓN DE LOS DIFERENTES ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO

English

DETERMINATION OF THE DIFFERENT ANALYTES RELATED TO SAMPLES FROM THE HUMAN ORGANISM

About this record

Access comprehensive regulatory information for 1. LIGHTMIX MODULAR ADENOVIRUS (1. LIGHTMIX MODULAR ADENOVIRUS) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 5ce0bdcca4ae369483d0aedd620fd6da and manufactured by TIB MOLBIOL SYNTHESELABOR GMBH. The device was registered on August 30, 2032.

This page provides complete registration details including product type (DIAGNOSTIC REAGENT), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.